A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4730233



Internal ID21401044
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:135127506..135269268hg38UCSC Ensembl
chrX:134261434..134403214hg19UCSC Ensembl
CytobandXq26.3
Allele length
AssemblyAllele length
hg38141763
hg19141781
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16258572, nssv16258478, nssv16256292, nssv16258728, nssv16255973, nssv16256261, nssv16257338, nssv16255861, nssv16258524, nssv16257619, nssv16256002, nssv16257856, nssv16257389, nssv16256905, nssv16256497, nssv16256051, nssv16255970, nssv16258186, nssv16258465, nssv16256867
SamplesNA19238, NA19239, HG00731, NA19240, HG00733
Known GenesCXorf48
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nsv4730233
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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